Mechanisms Flashcards
electrophilic addition of alkenes + bromine
.
room temp.
forms dihalogenoalkane
electrophilic addition of alkenes + sulfuric acid
.
room temp.
forms alcohol
electrophilic addition of alkenes + HBr
.
room temp.
forms halogenoalkane
elimination of halogenoalkanes & OH-
.
ethanolic/alcoholic
heat under reflux
forms alkene
elimination of alcohols (dehydration)
.
conc. sulfuric acid or conc. phosphoric acid catalyst
forms alkene
electrophilic addition for hydration of alkene
.
conc. phosphoric acid catalyst
H2O/aqueous
warm
forms alcohol
nucleophilic substitution of halogenoalkanes + OH-
.
aqueous
heat under reflux
forms alcohol
nucleophilic substitution of halogenoalkanes + CN-
.
KCN reagent
ethanolic & aqueous mixture
heat under reflux
forms nitrile
free radical substitution of alkanes + bromine
.
UV light
nucleophilic substitution of ammonia/amines
.
to form 1y only, excess conc. alcoholic NH3
to form 2y, 3y amines & 4y ammonium salt, excess halogenoalkane
nucleophilic addition of ketones/aldehydes + H-
.
NaBH4 –> H- aqueous
or LiAlH4 in ether
reduction
forms alcohol
nucleophilic addition of ketones/aldehydes + CN-
.
KCN/NaCN
dilute strong acid e.g. sulfuric acid
forms hydroxynitrile
nucleophilic addition-elimination of acyl chloride + water
.
H2O
room temp.
forms carboxylic acid
nucleophilic addition-elimination of acyl chloride + alcohol
.
alcohol
room temp.
forms ester
nucleophilic addition-elimination of acyl chloride + NH3
.
NH3
room temp.
forms 1y amide
nucleophilic addition-elimination of acyl chloride + 1y amine
.
1y amine
room temp.
forms 2y amide
electrophilic substitution of aromatic + NO2+
.
to form electrophile:
HNO3 + 2H2SO4 –> NO2+ + 2HSO4- + H3O+
conc. nitric acid & conc. sulfuric acid
forms nitro compounds
reduction of aromatic nitro compounds
(not mechanism)
Sn & mod. conc. HCl
electrophilic substitution of aromatic + acyl chloride/acid anhydride
.
formation of electrophile:
AlCl3 + CH3COCl –> CH3CO+ + AlCl4-
anhydrous AlCl3 catalyst